01 1H. Lundbeck AS
01 1LU AA24530 HYDROBROMIDE
01 1Denmark
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21844
Submission : 2008-09-29
Status : Inactive
Type : II
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PharmaCompass offers a list of Tedatioxetine Hydrobromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tedatioxetine Hydrobromide manufacturer or Tedatioxetine Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Tedatioxetine Hydrobromide API Price utilized in the formulation of products. Tedatioxetine Hydrobromide API Price is not always fixed or binding as the Tedatioxetine Hydrobromide Price is obtained through a variety of data sources. The Tedatioxetine Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tedatioxetine Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tedatioxetine Hydrobromide, including repackagers and relabelers. The FDA regulates Tedatioxetine Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tedatioxetine Hydrobromide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tedatioxetine Hydrobromide supplier is an individual or a company that provides Tedatioxetine Hydrobromide active pharmaceutical ingredient (API) or Tedatioxetine Hydrobromide finished formulations upon request. The Tedatioxetine Hydrobromide suppliers may include Tedatioxetine Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Tedatioxetine Hydrobromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tedatioxetine Hydrobromide DMF (Drug Master File) is a document detailing the whole manufacturing process of Tedatioxetine Hydrobromide active pharmaceutical ingredient (API) in detail. Different forms of Tedatioxetine Hydrobromide DMFs exist exist since differing nations have different regulations, such as Tedatioxetine Hydrobromide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tedatioxetine Hydrobromide DMF submitted to regulatory agencies in the US is known as a USDMF. Tedatioxetine Hydrobromide USDMF includes data on Tedatioxetine Hydrobromide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tedatioxetine Hydrobromide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tedatioxetine Hydrobromide suppliers with USDMF on PharmaCompass.
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